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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNF135
(R115K)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
RNF135
(A173G)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
RNF135
(Q301fs)
Deletion
(3 prime UTR variant +1 more)
not provided
GUncertain significance
RNF135
(D337N)
Single nucleotide variant
(3 prime UTR variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
RNF135
(W415C)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+1 more
GBenign/Likely benign
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